In this role, you will be responsible for maintaining and developing our Supplier Quality System to ensure compliance with GMP and pharmaceutical regulations. You will also lead a team of up to 8 professionals, playing a critical role in driving supplier qualification and quality processes across the organization.

Your responsibilities include, but are not limited to:

• Leading the Supplier Quality Team and managing supplier qualification processes.

• Organizing and participating in internal and external audits.
• Managing quality agreements with service and material providers.
• Handling supplier complaints and quality notifications.
• Reviewing and approving documentation in line with GMP, legal, and QAA requirements.
• Conducting internal training on GxP and quality assurance.
• Participating in audits and regulatory inspections at Polpharma Biologics.

If you have:

• Over 5 years of experience in pharmaceutical quality or related area.
• Higher education in a relevant field.
• Deep knowledge of GMP and pharmaceutical regulations.
• Fluency in English (both spoken and written).
• Excellent communication, problem-solving and documentation skills.
• Experience with analytical and manufacturing technologies related to medicinal products.

What we offer:

• Competitive salary.
• Private healthcare.
• Life insurance.
• Pension plan above national standards.
• Additional free day.
• and more..